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Biochimica Et Biophysica Acta|July 22, 2006
Identification and membrane localization of electrogenic sodium bicarbonate cotransporters in Calu-3 cellsJames L Kreindler, Kathryn W Peters, Raymond A Frizzell, et al.
The Journal of Biological Chemistry|August 9, 2008
An obligatory heterodimer of 14-3-3beta and 14-3-3epsilon is required for aldosterone regulation of the epithelial sodium channelXiubin Liang, Michael B Butterworth, Kathryn W Peters, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 28, 2007
Regulation of human cystic fibrosis transmembrane conductance regulator (CFTR) by serum- and glucocorticoid-inducible kinase (SGK1)J Denry Sato, M Christine Chapline, Renee Thibodeau, et al.
The Journal of Biological Chemistry|September 7, 2006
Derlin-1 promotes the efficient degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) and CFTR folding mutantsFei Sun, Ruilin Zhang, Xiaoyan Gong, et al.
The Journal of Biological Chemistry|January 8, 2016
VAMP-associated Proteins (VAP) as Receptors That Couple Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Proteostasis with Lipid HomeostasisWayne L Ernst, Kuntala Shome, Christine C Wu, et al.
The Journal of Biological Chemistry|December 3, 2015
Non-native Conformers of Cystic Fibrosis Transmembrane Conductance Regulator NBD1 Are Recognized by Hsp27 and Conjugated to SUMO-2 for DegradationXiaoyan Gong, Annette Ahner, Ariel Roldan, et al.
The Journal of Biological Chemistry|October 31, 2007
The deubiquitinating enzyme UCH-L3 regulates the apical membrane recycling of the epithelial sodium channelMichael B Butterworth, Robert S Edinger, Huib Ovaa, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 20, 2021
Separating the contributions of SLC26A9 and CFTR to anion secretion in primary human bronchial epitheliaMads B Larsen, Jeannie J Choi, Xiaohui Wang, et al.
Molecular Biology of the Cell|November 8, 2018
Different SUMO paralogues determine the fate of wild-type and mutant CFTRs: biogenesis versus degradationXiaoyan Gong, Yong Liao, Annette Ahner, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|March 4, 2008
Prostasin expression is regulated by airway surface liquid volume and is increased in cystic fibrosisMike M Myerburg, Erin E McKenna, Cliff J Luke, et al.
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